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Osteogenic Gene Transcription Is Regulated via Gap Junction-Mediated Cell-Cell Communication

机译:成骨基因转录是通过间隙连接介导的细胞间通讯来调节的

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An analytical study of cell-cell communications between murine osteoblast-like MLO-A5 cells and bone marrow mesenchymal stem cell (BMSC)-like C3H10T1/2 cells was performed. C3H10T1/2 cells expressing green fluorescent protein (10T-GFP cells) were generated to enable the isolation of the BMSC-like cells from co-cultures with MLO-A5 cells. The mRNA expression levels of several osteogenic transcription factors (Runx2, Osterix, Dlx5, and Msx2) did not differ between the co-cultured and mono-cultured 10T-GFP cells, but those of alkaline phosphatase (ALP) and bone sialoprotein (BSP) were 300- to 400-fold higher in the co-cultured cells. Patch clamp and biocytin transfer assays revealed gap junction-mediated communication between co-cultured 10T-GFP and MLO-A5 cells. The addition of a gap junction inhibitor suppressed the increases in the expression levels of the ALP and BSP mRNAs in co-cultured 10T-GFP cells. Furthermore, the histone acetylation levels were higher in co-cultured 10T-GFP cells than in mono-cultured 10T-GFP cells. These results suggest that osteoblasts and BMSCs associate via gap junctions, and that gap junction-mediated signaling induces histone acetylation that leads to elevated transcription of the genes encoding ALP and BSP in BMSCs.
机译:进行了鼠成骨细胞样MLO-A5细胞和骨髓间充质干细胞(BMSC)样C3H10T1 / 2细胞之间细胞间通讯的分析研究。产生了表达绿色荧光蛋白的C3H10T1 / 2细胞(10T-GFP细胞),从而能够从与MLO-A5细胞共培养物中分离出BMSC样细胞。在共培养和单培养的10T-GFP细胞之间,几种成骨转录因子(Runx2,Osterix,Dlx5和Msx2)的mRNA表达水平没有差异,但是碱性磷酸酶(ALP)和骨唾液蛋白(BSP)的mRNA表达水平没有差异。在共培养的细胞中,其高300-400倍。膜片钳和生物素转移测定揭示了共培养的10T-GFP和MLO-A5细胞之间的间隙连接介导的通讯。间隙连接抑制剂的添加抑制了共培养的10T-GFP细胞中ALP和BSP mRNA表达水平的增加。此外,共培养的10T-GFP细胞中的组蛋白乙酰化水平高于单培养的10T-GFP细胞。这些结果表明成骨细胞和BMSC通过间隙连接而缔合,并且间隙连接介导的信号传导诱导组蛋白乙酰化,从而导致BMSC中编码ALP和BSP的基因的转录升高。

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